Canonical Allele Identifier: CA920595207
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs1556160956

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12777946dup , CM000686.2:g.12777946dup GRCh38
NC_000024.9:g.14889880dup , CM000686.1:g.14889880dup GRCh37
NC_000024.8:g.13399274dup NCBI36
NG_008311.1:g.81721dup

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.2640-73dup ENSP00000498372.1:n.2640-73dup
ENST00000338981.7:c.2640-73dup MANE Select ENSP00000342812.3:n.2640-73dup
ENST00000426564.6:n.2652-73dup
NM_004654.3:c.2640-73dup NP_004645.2:n.2640-73dup
XM_011531469.1:c.2640-73dup XP_011529771.1:n.2640-73dup
XM_011531470.1:c.2406-73dup XP_011529772.1:n.2406-73dup
XM_017030078.2:c.2655-73dup XP_016885567.1:n.2655-73dup
NM_004654.4:c.2640-73dup MANE Select NP_004645.2:n.2640-73dup